Wolbachia 16S rRNA haplotypes detected in wild Anopheles stephensi in eastern Ethiopia

Background About two out of three Ethiopians are at risk of malaria, a disease caused by the parasites Plasmodium falciparum and Plasmodium vivax. Anopheles stephensi, an invasive vector typically found in South Asia and the Middle East, was recently found to be distributed across eastern and central Ethiopia and is capable of transmitting both P. falciparum and P. vivax. The detection of this vector in the Horn of Africa (HOA) coupled with widespread insecticide resistance requires that new methods of vector control be investigated in order to control the spread of malaria. Wolbachia, a naturally occurring endosymbiotic bacterium of mosquitoes, has been identified as a potential vector control tool that can be explored for the control of malaria transmission. Wolbachia could be used to control the mosquito population through suppression or potentially decrease malaria transmission through population replacement. However, the presence of Wolbachia in wild An. stephensi in eastern Ethiopia is unknown. This study aimed to identify the presence and diversity of Wolbachia in An. stephensi across eastern Ethiopia. Methods DNA was extracted from An. stephensi collected from eastern Ethiopia in 2018 and screened for Wolbachia using a 16S targeted PCR assay, as well as multilocus strain typing (MLST) PCR assays. Haplotype and phylogenetic analysis of the sequenced 16S amplicons were conducted to compare with Wolbachia from countries across Africa and Asia. Results Twenty out of the 184 mosquitoes screened were positive for Wolbachia, with multiple haplotypes detected. In addition, phylogenetic analysis revealed two superclades, representing Wolbachia supergroups A and B (bootstrap values of 81 and 72, respectively) with no significant grouping of geographic location or species. A subclade with a bootstrap value of 89 separates the Ethiopian haplotype 2 from other sequences in that superclade. Conclusions These findings provide the first evidence of natural Wolbachia populations in wild An. stephensi in the HOA. They also identify the need for further research to confirm the endosymbiotic relationship between Wolbachia and An. stephensi and to investigate its utility for malaria control in the HOA. Graphical Abstract Supplementary Information The online version contains supplementary material available at 10.1186/s13071-022-05293-9.

across eastern Ethiopia [5]. It has been demonstrated that An. stephensi is capable of transmitting both P. falciparum and P. vivax in eastern Ethiopia and the establishment of this vector could increase the prevalence of P. falciparum cases by 50% in areas found to be suitable if no additional intervention occurs [6,7]. With the knowledge that An. stephensi can transmit both Plasmodium species in eastern Ethiopia, strategies for the control or elimination of An. stephensi in the HOA are being investigated. Insecticide resistance has already been identified in An. stephensi in eastern Ethiopia [8,9], requiring alternative methods of vector control such as the use of Wolbachia pipientis.
Wolbachia pipientis, more commonly referenced as Wolbachia, is an endosymbiotic bacterium of invertebrates that is classified into different supergroups based on major phylogenetic diversions. All Wolbachia in mosquitoes belong to supergroups A and B [10]. Wolbachia has been identified as a resource to address vectorborne diseases in Aedes mosquitoes through two main methods: population suppression [11] and population replacement [12,13]. Both methods are based on the mechanism of cytoplasmic incompatibility (CI). When an uninfected female mosquito mates with a male mosquito infected with Wolbachia, embryonic death occurs, and the female's larvae are inviable. In population suppression, male mosquitoes infected with Wolbachia are released on a large scale to decrease the population size, thus decreasing the transmission of vector-borne diseases. Population replacement involves releasing both male and female mosquitoes with Wolbachia infection into a population of Wolbachia-free, disease-carrying mosquitoes [14].
Generally, the relationship between Wolbachia infection and Plasmodium infection in field Anopheles species is not well studied. Kambris et al. [15] and Hughes et al. [16] have shown that in the lab, Anopheles gambiae can be infected with wMelPop and wAlbB, and that Plasmodium berghei and P. falciparum development is inhibited with both Wolbachia strains. In field populations of Anopheles coluzzii and An. gambiae, Shaw et al. [17] and Gomes et al. [18] demonstrated that Wolbachia infection correlated negatively with Plasmodium development. This is indicative of potential for Wolbachia-based interventions, but more research is needed.
In An. stephensi specifically, Wolbachia infections in lab populations have been briefly studied. Bian et al. [19] were able to stably infect An. stephensi with wAlbB. They showed that maternal transmission and CI induction were successful, and observed resistance to P. falciparum infection in the lab strain of An. stephensi. Chen et al. [20] showed that An. stephensi can be stably infected by wAlbB and that there was no change in the microbiome of the mosquitoes upon Wolbachia infection. These results indicate that lab strains of An. stephensi can hold stable infections of Wolbachia, which may mean that field populations are susceptible to infection, although further research is needed [18].
The limited study of Wolbachia infection in An. stephensi has mainly been in lab populations. We need to determine whether Wolbachia infection is present in order to begin evaluating the potential of Wolbachiabased control strategies for malaria transmission in An. stephensi in eastern Ethiopia. Furthermore, the strain of Wolbachia in the wild host population needs to be determined, to establish which population control strategy would function best, should a validated Wolbachiabased malaria control tool become achievable [13]. Wolbachia is typically detected via DNA or RNA extraction from the host invertebrate and targeting multiple genes to determine infection. These genes include the 16S-encoding gene, the surface protein-encoding gene (Wolbachia surface protein [wsp]), and the five multilocus strain typing (MLST) genes (ftsZ, fbpA, hcpA, coxA, and gatB) [10]. Previous studies have depended solely on Wolbachia 16S for confirming infection [18,19]; however, more recent research has indicated that multiple genes must be detected in order to confirm infection [20]. Very few Anopheles species have been screened for Wolbachia, with proven infection occurring only in two highly diverged species in sub-Saharan Africa [21]. There has also been significant difficulty in many studies with amplifying the genes in MLST. Gomes et al. were only able to amplify three out of five genes, and Jeffries et al. were unable to amplify any MLST genes in multiple sample groups [18,20]. This may indicate that environmental contamination is present or that divergence among these genes has emerged, precluding the use of the standard MLST primer set [18,22,23].
Since the detection of An. stephensi in the HOA, no investigation regarding the possibility of Wolbachia endosymbiosis has been conducted in this population. One study surveyed An. stephensi for Wolbachia in Tamil Nadu, India, and reported the detection of 16S Wolbachia DNA in a portion of their mosquitoes [24]. Still, more information is needed to confirm whether Wolbachia is a true endosymbiont of An. stephensi, as Wolbachia in An. stephensi in the Middle East and the rest of South Asia has not been investigated.
In order to evaluate Wolbachia as a potential control method for malaria transmission, we first need to know whether Wolbachia is present in An. stephensi in eastern Ethiopia. In addition, the detection of Wolbachia DNA could provide a basis for using it in the complementary phylogeographic analysis of the An. stephensi invasion. In this study, we used Wolbachia 16S ribosomal RNA (rRNA)-, wsp-, and MLST-targeted polymerase chain reaction (PCR) assays to detect Wolbachia in An. stephensi from eastern Ethiopia.

Sampling of An. stephensi
Anopheles stephensi surveys were conducted from August through November 2018 in Semera, Godey, Kebridehar, Erer-Gota, and Dire Dawa. Details about the collection sites and approach have been described previously [5]. Briefly, adult mosquitoes were collected via pyrethrum spray catch (PSC) and Centers for Disease Control and Prevention (CDC) light traps. The collected mosquitoes were sorted between culicines and Anopheles, and the latter were further sorted to distinguish An. stephensi from other Anopheles species using a standard morphological key [25] and a key prepared by Coetzee (subsequently published in 2020 [26]). Analysis of Plasmodium detection was conducted previously, and no wild-caught adult mosquitoes contained Plasmodium falciparum or P. vivax DNA [5].
Larvae and pupae of Anopheles were also collected from larval habitats including artificial water storage containers, freshwater pools, discarded tires, and plastic containers. Larvae were reared in field insectaries using water taken from larval habitats, feeding them with baker's yeast and exposing them to sunlight during the day. Pupae were transferred into adult emergence cages and adults were morphologically identified using the same keys [25,26]. The numbers of wild-caught adults and reared larvae are documented in Additional file 1: Table S1.

DNA extraction and molecular identification of mosquitoes
DNA was extracted from either the abdomens or whole bodies of An. stephensi mosquitoes, selected at random, using the DNeasy Blood & Tissue Kit (Qiagen, Valencia, CA, USA). PCR was performed for each individual mosquito, targeting the nuclear internal transcribed spacer 2 (ITS2) region and the mitochondrial cytochrome c oxidase subunit 1 (COI). The reagent components and final concentrations for the PCR assays were 1× Promega Hot Start Master Mix (Promega, Madison, WI, USA) and 0.5 mM for both primers, plus 1 µl of isolated DNA template. A region including the ITS2 gene was amplified via PCR using universal primers as described previously [27]. Updated annotations show that identification via these primers is based on a portion of the sequence that includes 28S in the ITS2 assay [28]. The PCR temperature protocol consisted of 95 °C for 1 min, 30 cycles of 95 °C for 30 s, 48 °C for 30 s, and 72 °C for 1 min; followed by 72 °C for 10 min. All samples successfully amplified ITS2. A region including the COI gene was amplified via PCR using universal primers as described previously [3]. The PCR temperature protocol consisted of 95 °C for 1 min, 30 cycles of 95 °C for 30 s, 48 °C for 30 s, and 72 °C for 1 min; followed by 72 °C for 10 min.

Molecular Wolbachia detection
The Wolbachia 16S rRNA-encoding gene (16S), and the Wolbachia surface protein encoding gene (wsp) were amplified to detect Wolbachia in the mosquitoes. A positive control of extracted genomic DNA from Wolbachiainfected Drosophila melanogaster (provided by The Wolbachia Project at Vanderbilt University) was used to troubleshoot PCR protocols and ensure the PCR successfully amplified Wolbachia 16S, wsp, and the genes within MLST. A negative control of no genomic DNA (gDNA) template was used to ensure no contamination of the PCR reagents. The reagent components and final concentrations for the PCR assays were 1X Promega Hot Start Master Mix (Promega, Madison, WI, USA) and 0.4 mM for each primer 16S and wsp, plus 4 µl and 2 µl of isolated DNA template for Wolbachia 16S, and wsp, respectively. For the 16S assay, a nested protocol was used.
The first set of Wolbachia 16S primers, as described in Werren and Windsor, amplified an un-nested 438-basepair (bp) fragment [29]. The PCR cycling protocol was as follows: 95 °C for 2 min, 2 cycles of 95 °C for 1 min, 60 °C for 1 min, and 72 °C for 1 min, followed by 35 cycles of 95 °C for 30 s, 60 °C for 1 min, and 72 °C for 45 s, and lastly 72 °C for 5 min. For the nested reaction, specific internal primers were used as described by Shaw et al., which amplified a 412-bp fragment [17]. Two microliters of PCR product from the un-nested reaction was used in this reaction as template DNA. The PCR temperature protocol was as follows: 95 °C for 15 min, 35 cycles of 95 °C for 15 s, 66 °C for 25 s, and 72 °C for 30 s, followed by 72 °C for 5 min.
For the wsp assay, a 546 bp region including the gene was amplified using primers as described in Zhou et al. [30]. The PCR temperature protocol was as follows: 94 °C for 2 min, then 35 cycles of 94 °C for 1 min, 55 °C for 1 min, and 72 °C for 1 min; followed by 72 °C for 5 min. All primers used are listed in Additional file 1: Table S2. All PCR products were run on a 2% agarose gel, and the gel was visualized using a Gel Doc EZ imager (Bio-Rad Laboratories, Inc., Hercules, CA, USA) prior to Sanger sequencing by a commercial laboratory (Eurofins Genomics LLC).

Multilocus strain typing
In addition to amplifying the 16S and wsp genes, MLST was performed on each 16S-positive sample to determine whether the Wolbachia infection was present. Five loci, including ftsZ, fbpA, hcpA, coxA, and gatB, were tested, using region-specific primers. The ftsZ universal assay amplified a 775 bp region [31], the fbpA assay amplified 429 bp, the hcpA assay amplified a 444 bp region, the coxA assay amplified a 402 bp region, and the gatB assay amplified a 369 bp region [10]. A nested protocol was used for all five MLST genes. The hcpA, fbpA, and gatB nested assays were used as previously described on the PubMLST website [32]. Two microliters of PCR product from the un-nested reaction was used in this reaction as template DNA. Nested PCR cycling conditions were as follows: 95 °C for 15 min, 50 cycles of 95 °C for 15 s, 55 °C for 30 s, and 72 °C for 1 min; followed by 72 °C for 5 min. The ftsZ and coxA nested assays were used as described previously and amplified products 424 bp and 357 bp in length, respectively [33]. The nested PCR protocol for ftsZ and coxA consisted of 94 °C for 5 min, 36 cycles of 94 °C for 15 s, 55 °C for 15 s, and 72 °C for 30 s; followed by 72 °C for 10 min. All primers used are listed in Additional file 1: Table S2. All PCR products were run on a 2% agarose gel, and the gel was visualized using a Gel Doc EZ imager (Bio-Rad Laboratories, Inc., Hercules, CA, USA).

Sequence and phylogenetic analysis
Sequences were cleaned and analyzed using Codon-Code (CodonCode Corporation, Centerville, MA, USA). Wolbachia 16S, Wolbachia coxA, and An. stephensi COI sequences were submitted as queries to the National Center for Biotechnology Information's (NCBI) Basic Local Alignment Search Tool (BLAST) against the nucleotide collection under standard parameters (100 max target sequences, expect threshold 0.05, word size 28, optimized for highly similar sequences, not specific to any organism). This information was used to confirm that the amplicons produced were the Wolbachia 16S gene, Wolbachia coxA gene, or An. stephensi COI. An alignment of observed haplotypes and the nucleotide conservation in the An. stephensi Wolbachia 16S sequences were visualized on CLC Sequence Viewer 7.6 (CLC Bio Qiagen, Aarhus, Denmark).
Phylogenetic analysis was performed with the representative 16S sequences collected from this study, as well as peer-reviewed, published Wolbachia 16S sequences from NCBI GenBank in anopheline mosquitoes with an outgroup of Rickettsia japonica (Additional file 1: Table S3) [18,19,[33][34][35][36][37][38]. Phylogenetic analysis was also performed with the coxA sequences collected from this study, as well as peer reviewed, published Wolbachia coxA sequences from NCBI GenBank in anopheline mosquitoes with an outgroup of the Wolbachia endosymbiont of Dirofilaria immitis (Additional file 1: Table S3) [18,33,36]. An additional phylogenetic analysis was performed with the Wolbachia 16S sequences from sub-Saharan Africa used in the first analysis, the three 16S haplotypes collected in this study, and four 16S sequences from a study in pre-print from Tamil Nadu, India (Additional file 1: Table S3) [18,24,33,36]. Lastly, phylogenetic analysis was performed on the COI genes from the An. stephensi that were Wolbachia 16S-positive, with an outgroup of Anopheles maculatus (Additional file 1: Table S3). Representative sequences from each location were determined by aligning sequences and eliminating non-distinct haplotypes. Alignments were created with MAFFT version 7 [39] and trimmed to 283 bp (16S; Fig. 2), 323 bp (16S; Additional file 1: Fig. S1), 357 bp (coxA; Fig. 3), and 321 bp (COI; Fig. 4) using Mesquite version 3.61 [40]. Phylogenetic associations between all sequences were estimated using a maximum likelihood approach with RAxML [41]. The GTRGAMMA option that utilizes the general time-reversible (GTR) model of nucleotide substitution with the gamma model of the rate of heterogeneity was used. A total of 1000 runs were completed using the maximum likelihood criteria with rapid bootstrap analysis. The RAxML output was viewed in FigTree [42] with a root at the outgroup and transformed branches, and a phylogenetic tree image was made.

Wolbachia detected in four of five survey sites
A total of 184 mosquito samples were tested, with 20 samples testing positive for Wolbachia 16S DNA in the nested PCR (Table 1). Two of these 20 samples were from wild-caught adult mosquitoes, whereas 18 were from laboratory-reared adults. Out of the 20 samples, seven samples were also positive in the un-nested PCR reaction ( Table 2). The highest prevalence was found in Godey and Semera. One sample tested positive for Wolbachia coxA in the nested PCR reaction. No positives were detected using the wsp gene or the four other MLST genes.
Haplotypes 1 and 2 are the most similar, with 3 being more differentiated (16 nucleotide differences). Haplotype 3 has the highest number of single nucleotide substitutions or deletions in comparison with haplotypes 1 and 2. Even though there is a significant difference between haplotype 3 and haplotypes 1 and 2, most (94.33%) of the 16S gene is conserved (Fig. 1a).

Wolbachia 16S in An. stephensi falls into multiple clades
Phylogenetic analysis revealed two superclades with bootstrap values of 81 and 72 representing Wolbachia supergroups A and B, respectively. Haplotype 3 only occurs in supergroup B, while haplotypes 1 and 2 occur in supergroup A. One of these superclades had a subclade composed of just haplotype 2 sequences from Ethiopia and received significant support separating this clade from the rest of the superclade (bs = 89). The Wolbachia 16S sequences from Ethiopia were in clades with sequences from both Africa and SE Asia and multiple Anopheles species. Overall, there was no clear clustering by geography or species (Fig. 2).

Wolbachia coxA in eastern Ethiopia confirms the presence of Wolbachia in supergroup B
Out of the five MLST genes, cytochrome c oxidase subunit 1 (coxA) was the only gene to be amplified, in the sample SM006. This sample is the only sample we found in supergroup B, and is the most distinguished haplotype, haplotype 3. We were able to amplify this  Total 7 20 Fig. 1 a Alignment of the three haplotypes observed from the Wolbachia 16S gene in eastern Ethiopia. Haplotypes were categorized as 1, 2, and 3. Nucleotide conservation is indicated by a gray bar below the alignment. b Haplotype frequency per collection site gene three times from the same sample. Phylogenetic analysis showed that the sample from Ethiopia is significantly differentiated from the rest of the tree and clusters with samples known to be in supergroup B (Fig. 3).

Wolbachia in An. stephensi from India falls into the same clade as haplotype 3 from eastern Ethiopia
To investigate whether Wolbachia in An. stephensi in eastern Ethiopia is similar to that found in the Middle East and South Asia, we performed a phylogenetic analysis of Wolbachia 16S sequences from Tamil Nadu, India, to those of eastern Ethiopia and sub-Saharan Africa. We again see separation into supergroups A and B. Supergroup B is represented in the top superclade and supergroup A is represented in the bottom superclade. The sample that is the strongest candidate for infection clusters with the sequences from India in supergroup B, but the sequences were not the same (Additional file 1: Fig. S1).

Wolbachia 16S diversity and An. stephensi COI diversity
To investigate any correlation between Wolbachia diversity and An. stephensi diversity, we amplified the COI gene in all of our Wolbachia 16S-positive mosquitoes. The sample from Semera presents both the most COI diversity and the most Wolbachia 16S diversity. This is consistent with previous reports of mitochondrial diversity in the An. stephensi in eastern Ethiopia [5]. Samples from Semera (SM) occur in all three major clades in this tree. More southern sites, such as Godey (GD) and Kebridehar (KB), are in the topmost clade, and more northern and central sites such as Dire Dawa (DD) and Semera are mostly in the bottom two clades (Fig. 4). While we are unable to say that this pattern is Fig. 2 Phylogenetic tree of Wolbachia 16S in Anopheles species, with transformed branches. There were two major clades separated by significant bootstrap values 72 and 81. A subclade including haplotype 2 sequences from eastern Ethiopia was found to have significant support to be separate from the rest of the superclade. No geographic or species-specific clustering was found. The outlier sequence MH596695 did not follow the clustering of Wolbachia supergroup A or B, so it was not included in the distinction between these supergroups. Rickettsia japonica was used as the outgroup (NR074459). Haplotype 1 is designated by light blue font, haplotype 2 is designated by red font, and haplotype 3 is designated by orange font definitive based on our sample size, we predict that if we were to obtain a larger sample set, we would see this trend separate our samples out more distinctively.

Discussion
The data presented here confirm Wolbachia 16S rRNA molecular detection in An. stephensi and provide preliminary evidence of Wolbachia infection in this species. Wolbachia 16S DNA was detected in about 10% of samples across all collection sites. Three haplotypes were detected across all the sites with Wolbachia 16S-positive samples. Haplotypes 1 and 2 (supergroup A) were the most similar, with haplotype 3 (supergroup B) being the most dissimilar. Haplotype 2 was the most predominant haplotype, with 11 samples. Semera presented with the most diversity, exhibiting all three haplotypes. It should be noted that the number of positive Wolbachia samples was relatively low at each site, thus conclusions about the correlation between geographic location in Ethiopia and Wolbachia 16S diversity should be followed up with a larger sample set. Detection of Wolbachia coxA confirmed one of our samples, SM006, as a part of supergroup B. This provides an additional line of evidence of infection in the case of sample SM006, as most contamination scenarios can be eliminated.
Phylogenetic analysis revealed no significant clustering of Wolbachia 16S rRNA sequences with host Anopheles species or geographical regions. We predicted that there may be clustering of Wolbachia 16S based on geographic region or relatedness of the vector, but this was not observed. Phylogenetic analysis also revealed no significant relationship between Wolbachia 16S in India and that of eastern Ethiopia. Thus, there does not appear to be any specificity of 16S haplotype to Anopheles species or geographic region. Lastly, phylogenetic analysis of An. stephensi COI colored by Wolbachia 16S haplotype revealed possible patterns of Wolbachia diversity. There is separation between southeastern Ethiopia and central/ northeastern Ethiopia. Most of the sequences in Wolbachia 16S haplotype 1 appear in southeastern Ethiopia and most of the sequences in Wolbachia 16S haplotype 2 appear in central/northeastern Ethiopia. More samples would be needed in order to confirm any patterns observed.
The prevalence of detection found here is similar to that found in a study of the An. gambiae complex in Guinea, which was around 11% in Anopheles melas via MLST [20]. The authors of that study suggested that using a nested 16S approach is problematic, citing a study investigating the presence of Wolbachia 16S in the An. Fig. 3 Phylogenetic tree of Wolbachia coxA in Anopheles species in sub-Saharan Africa, as well as Wolbachia strains from Culex pipiens and Drosophila melanogaster with transformed branches. We do not see separation into different supergroups; however, the sample from Ethiopia is significantly differentiated from the rest of the tree and clusters with samples known to be in supergroup B. Supergroup C Wolbachia from Dirofilaria immitis was used as the outgroup (KU255267). The sample from Ethiopia is designated in orange gambiae genome. The authors discussed the establishment of the nested 16S PCR protocol, and how it produces unreliable and non-replicable results [22]. We see in our study that only seven out of 20 total 16S-positive samples showed a band in the un-nested PCR. All quality sequences were produced from nested PCR products, which raises the question of whether nested PCR should be used to determine Wolbachia infection.
The density of infection is currently unknown in Anopheles species. In a previous study, infections found in An. demeilloni and An. moucheti were described as high-density; however, corresponding data show Wolbachia 16S representing from less than 20% to just over 80% of the total microbiome. This indicates that densities in a species could vary, which would mean that the nested protocol may need to be used in the case of lowerdensity infections or co-infection with another bacterium such as Asaia [20]. As this method does not provide a clear measure of the number of bacteria, we suggest incorporating quantitative PCR (qPCR) and fluorescence in situ hybridization (FISH) in the future.
Questions about whether the detection of Wolbachia DNA in An. stephensi populations from this study is indicative of an actual infection can be further examined by comparing the diversity of the Wolbachia detected in the recently introduced population of An. stephensi in Ethiopia to Wolbachia detected in long-established An. stephensi populations. As an endosymbiont of invasive mosquitoes, the Wolbachia population should mirror a lower level of diversity in its invasive host population Fig. 4 Phylogenetic analysis of An. stephensi COI in the Wolbachia 16S-positive An. stephensi with transformed branches. Each sample is colored by Wolbachia haplotype, where haplotype 1 is colored in blue, haplotype 2 is colored in red, and haplotype 3 is colored in yellow. Haplotypes 1 and 2 are representative of Wolbachia supergroup A, and haplotype 3 is representative of supergroup B. Anopheles stephensi COI haplotypes are designated on the clades that they represent according to Carter et al. [45]. Anopheles maculatus was used as an outgroup (KT382822). The sample sites are abbreviated as follows: Semera (SM), Dire Dawa (DD), Godey (GD), and Kebridehar (KB). Only 19 An. stephensi samples amplified COI, which was likely due to sequence divergence in the COI region in that mosquito relative to the corresponding host source population [43,44]. A study in pre-print from the state of Tamil Nadu, India, detected four haplotypes of Wolbachia 16S, and in eastern Ethiopia we detected three haplotypes. While the SM006 sequence was found in supergroup B that also included the India sequences, we did not have enough sequence resolution to provide definitive evidence of a shared recent ancestor between An. stephensi Wolbachia from Ethiopia and India. Further testing would require additional sampling and congruent multilocus genetic data.
There are limitations to using only a PCR assay for detection. Multiple studies have been published regarding Wolbachia infection and the detection of 16S, wsp, and MLST. Jeffries et al. [20] discussed how extracting RNA from the mosquitoes would increase the chance of detecting actively expressed Wolbachia genes. This could increase the effectiveness of the PCR assays, as they would amplify actively expressed genes rather than the scenarios below. A recent systematic review discussed the different scenarios in which Wolbachia could be detected in a mosquito [23]. The authors pointed out that under scenarios such as a mosquito with an endogenized gene from Wolbachia, environmental contamination, or a mosquito infected with a nematode infected with Wolbachia, Wolbachia would be detectable by PCR assay, nested PCR assay, qPCR, and possibly MLST. Additional scenarios were discussed in Chrostek and Gerth [22], where Wolbachia sequences could be detected in the gut as a result of the consumption of Wolbachia-infected food. In this study, we are able to rule out the scenario in which the mosquitoes were infected with a nematode that was infected with Wolbachia, as filarial worms are infected with Wolbachia in supergroups C and D. Environmental contamination is a possibility, as Aedes spp. share similar breeding habits with An. stephensi in eastern Ethiopia. However, other mosquitoes have not been tested for Wolbachia in eastern Ethiopia, so we cannot rule this out. For sample SM006, the integration of a Wolbachia gene into the host genome is unlikely, as it is not likely that multiple genes would integrate into the host genome [23]. In the scenario that a mosquito is infected with Wolbachia, methods such as FISH, transmission electron microscopy (TEM), and Giemsa staining (GIEMSA) must be used to detect the active Wolbachia in the ovaries [23]. This suggests that future studies aiming to detect Wolbachia in mosquitoes should aim to perform one of these visual methods in addition to molecular assays.
If the detection of Wolbachia 16S and coxA represents true infection, then our findings provide helpful information about the strains present in An. stephensi in eastern Ethiopia. These are helpful data that can inform the approach to malaria control, should Wolbachia-based strategies in Anopheles become a reality [13]. Insecticide resistance has been identified in An. stephensi to pyrethroids, carbamates, and organophosphates, suggesting the need for alternative methods of vector control to prevent the prevalence of malaria from increasing [8,9]. Identifying the presence of Wolbachia 16S and coxA DNA in this invasive vector in eastern Ethiopia warrants further studies, including methods such as reverse transcription qPCR and FISH.

Conclusions
In this study, we present the first evidence suggesting the presence of a Wolbachia population in An. stephensi in eastern Ethiopia. The detection of Wolbachia 16S and coxA DNA in An. stephensi in Ethiopia supports the need for further investigation of natural Wolbachia infections in this species. This could help inform the development of novel approaches for preventing the spread of malaria resulting from this invasive species in the HOA.